Canonical Allele Identifier: CA1096292576

Gene: ARID1B

Linked Data

• dbSNP Id: rs1789969323
• gnomAD v3: 6-157148595-GCTTTA-G
• gnomAD v4: 6-157148595-GCTTTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148600_157148604del , CM000668.2:g.157148600_157148604del	GRCh38
NC_000006.11:g.157469734_157469738del , CM000668.1:g.157469734_157469738del	GRCh37
NC_000006.10:g.157511426_157511430del	NCBI36
NG_032093.1:g.375671_375675del
NG_032093.2:g.375671_375675del
NG_066624.1:g.377575_377579del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-24_2762-20del	ENSP00000055163.8:n.2762-24_2762-20del
ENST00000414678.8:c.2672-24_2672-20del	ENSP00000412835.3:n.2672-24_2672-20del
ENST00000637015.2:c.2762-24_2762-20del	ENSP00000489729.2:n.2762-24_2762-20del
ENST00000319584.11:c.776-24_776-20del	ENSP00000313006.7:n.776-24_776-20del
ENST00000346085.10:c.2801-24_2801-20del	ENSP00000344546.5:n.2801-24_2801-20del
ENST00000350026.10:c.2513-24_2513-20del	ENSP00000055163.7:n.2513-24_2513-20del
ENST00000414678.7:c.920-24_920-20del	ENSP00000412835.2:n.920-24_920-20del
ENST00000452544.2:n.663-24_663-20del
ENST00000635849.1:c.83-24_83-20del	ENSP00000490948.1:n.83-24_83-20del
ENST00000636930.2:c.2762-24_2762-20del MANE Select	ENSP00000490491.2:n.2762-24_2762-20del
ENST00000637810.1:c.263-24_263-20del	ENSP00000489636.1:n.263-24_263-20del
ENST00000637904.1:c.263-24_263-20del	ENSP00000490550.1:n.263-24_263-20del
ENST00000647938.1:c.2552-24_2552-20del	ENSP00000498155.1:n.2552-24_2552-20del
ENST00000674190.1:n.1511-24_1511-20del
ENST00000319584.10:c.779-24_779-20del	ENSP00000313006.6:n.779-24_779-20del
ENST00000346085.9:c.2552-24_2552-20del	ENSP00000344546.4:n.2552-24_2552-20del
ENST00000350026.9:c.2513-24_2513-20del	ENSP00000055163.7:n.2513-24_2513-20del
ENST00000414678.6:c.920-24_920-20del	ENSP00000412835.2:n.920-24_920-20del
ENST00000452544.1:n.609-24_609-20del
NM_017519.2:c.2513-24_2513-20del	NP_059989.2:n.2513-24_2513-20del
NM_020732.3:c.2552-24_2552-20del	NP_065783.3:n.2552-24_2552-20del
XM_005267069.3:c.2513-24_2513-20del	XP_005267126.2:n.2513-24_2513-20del
XM_011535984.1:c.1463-24_1463-20del	XP_011534286.1:n.1463-24_1463-20del
XM_011535985.1:c.1283-24_1283-20del	XP_011534287.1:n.1283-24_1283-20del
XM_011535986.1:c.1043-24_1043-20del	XP_011534288.1:n.1043-24_1043-20del
XM_011535987.1:c.662-24_662-20del	XP_011534289.1:n.662-24_662-20del
XM_011535988.1:c.-20+15393_-20+15397del	XP_011534290.1:n.-20+15393_-20+15397del
NM_001346813.1:c.2513-24_2513-20del	NP_001333742.1:n.2513-24_2513-20del
NM_001363725.1:c.263-24_263-20del	NP_001350654.1:n.263-24_263-20del
XM_011535984.2:c.2594-24_2594-20del	XP_011534286.2:n.2594-24_2594-20del
XM_011535988.3:c.-20+15393_-20+15397del	XP_011534290.1:n.-20+15393_-20+15397del
XM_017011103.2:c.2594-24_2594-20del	XP_016866592.1:n.2594-24_2594-20del
XM_017011104.1:c.2594-24_2594-20del	XP_016866593.1:n.2594-24_2594-20del
XM_017011105.2:c.2594-24_2594-20del	XP_016866594.1:n.2594-24_2594-20del
XM_017011106.2:c.2594-24_2594-20del	XP_016866595.1:n.2594-24_2594-20del
XM_017011107.2:c.2414-24_2414-20del	XP_016866596.1:n.2414-24_2414-20del
XR_002956289.1:n.2677-24_2677-20del
NM_001363725.2:c.263-24_263-20del	NP_001350654.1:n.263-24_263-20del
NM_001371656.1:c.2801-24_2801-20del	NP_001358585.1:n.2801-24_2801-20del
NM_001374820.1:c.2801-24_2801-20del	NP_001361749.1:n.2801-24_2801-20del
NM_001374828.1:c.2762-24_2762-20del MANE Select	NP_001361757.1:n.2762-24_2762-20del
NM_017519.3:c.2762-24_2762-20del	NP_059989.3:n.2762-24_2762-20del